IP Library Granted Patent US 10,997,871
Granted Patent B2
US 10,997,871 · App. 15/514,011 · Granted May 4, 2021

Contractile function measuring devices, systems, and methods of use thereof

Inventors: Kevin Kit Parker (Cambridge, MA); Sung-Jin Park (Lexington, MA); Patrick Healy Campbell (Marlborough, MA); Johan Ulrik Lind (Boston, MA)
Assignee: President and Fellows of Harvard College
G09B23/28C12M21/08C12M25/02C12M31/10C12M41/46C12N5/0657G01N3/32G01N33/5091G01N2203/0089
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Quick Facts
Patent No.
US 10,997,871
App. No.
15/514,011
Granted
May 4, 2021
Kind
B2
Abstract

Exemplary embodiments provide systems, devices and methods for simultaneously measuring mechanical and electrophysiological tissue responses (e.g., contractile function, or the like).

Claims (21)

1. A method of measuring a contractile function, comprising:

providing a device comprising (i) a support structure, (ii) a mechanical sensor system, and (iii) an electrophysiological sensor system;

positioning a tissue structure on the support structure, said tissue structure comprising one or more intracellular electrodes and/or extracellular electrodes;

electrically stimulating the tissue structure to cause contractile function of the tissue structure; and

simultaneously measuring a mechanical activity associated with contraction of the tissue structure with the mechanical sensor system and an electrophysiological activity associated with contraction of the tissue structure with the electrophysiological sensor system.

2. The method of claim 1 , wherein the tissue structure comprises at least one of a flexible polymer layer or a hydrogel layer, and a population of isolated muscle cells expressing a photosensitive membrane transport mechanism seeded on at least one of the flexible polymer layer or the hydrogel layer in a predetermined pattern.

3. The method of claim 1 , further comprising stimulating the tissue structure with a light source providing photostimulation to the tissue structure, the photostimulation resulting in a contractile function of the tissue structure.

4. The method of claim 3 , wherein the photostimulation is provided to the tissue structure at specific wavelengths of light and specific optical pacing frequencies to control contraction of the tissue structure to mimic normal tissue or diseased tissue.

5. The method of claim 3 , wherein stimulating the tissue structure with the light source providing the photostimulation to the tissue structure comprises providing the photostimulation to the tissue structure in a predetermined spatiotemporal pattern of light with the light source.

6. The method of claim 5 , wherein providing the photostimulation to the tissue structure in the predetermined spatiotemporal pattern of light with the light source comprises:

illuminating a first portion of the tissue structure with a first set of optical pulses at a substantially constant frequency; and

illuminating a second portion of the tissue structure with an additional optical pulse for cross-field stimulation, a temporal interval between a pulse in the first set of optical pulses and the additional optical pulse resulting in a spiral wave pattern of contraction.

7. The method of claim 5 , wherein providing the photostimulation to the tissue structure in the predetermined spatiotemporal pattern of light with the light source comprises:

illuminating a first portion of the tissue structure along a line with a first set of optical pulses at a substantially constant frequency;

illuminating a second portion of the tissue structure with a first additional optical pulse for cross-field stimulation with a first temporal interval between a pulse in the first set of optical pulses and the first additional optical pulse; and

illuminating the second portion of the tissue structure with a second additional optical pulse for cross-field stimulation with a second temporal interval between a pulse in the first set of optical pulses and the first additional optical pulse.

8. The method of claim 7 , further comprising determining a temporal interval vulnerability window based on whether each additional optical pulse resulted in a spiral wave pattern of contraction.

9. The method of claim 8 , wherein providing the photostimulation to the tissue structure in the predetermined spatiotemporal pattern of light with the light source comprises:

illuminating a first portion of the tissue structure along a line with sets of optical pulses at a substantially constant frequency; and

illuminating a second portion of the tissue structure with additional optical pulses for cross-field stimulation, a temporal interval between a pulse in the sets of optical pulses and the subsequent additional optical pulse varying for each subsequent additional optical pulse.

10. The method of claim 1 , wherein simultaneously measuring the electrophysiological activity associated with contraction of the tissue structure with the electrophysiological sensor system comprises optically measuring an intensity or spectrum of (i) a synthetic indicator or (ii) a genetically encoded fluorescent protein indicator due to change in membrane voltage and in ion concentration of tissue in the tissue structure with the electrophysiological sensor system.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2021
From: CAMPBELL, PATRICK H.; LIND, JOHAN ULRIK; PARK, SUNG-JIN; PARKER, KEVIN KIT
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 054885/0557 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2017
From: CAMPBELL, PATRICK H.; LIND, JOHAN ULRIK; PARK, SUNG-JIN; PARKER, KEVIN KIT
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 041750/0084 →
CONFIRMATORY LICENSE Recorded Mar 27, 2017
From: HARVARD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042098/0159 →
Continuity (2)
Provisional Application 62054627 · Sep 24, 2014
Related Publication 20180357927A1 · Dec 13, 2018